CN109762454A - A kind of preparation method of automobile varnish Si modification double-component waterborne polyurethane composite coating - Google Patents
A kind of preparation method of automobile varnish Si modification double-component waterborne polyurethane composite coating Download PDFInfo
- Publication number
- CN109762454A CN109762454A CN201910094774.8A CN201910094774A CN109762454A CN 109762454 A CN109762454 A CN 109762454A CN 201910094774 A CN201910094774 A CN 201910094774A CN 109762454 A CN109762454 A CN 109762454A
- Authority
- CN
- China
- Prior art keywords
- component
- composite coating
- waterborne polyurethane
- agent
- double
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 40
- 239000011248 coating agent Substances 0.000 title claims abstract description 35
- 239000002131 composite material Substances 0.000 title claims abstract description 34
- 230000004048 modification Effects 0.000 title claims abstract description 30
- 238000012986 modification Methods 0.000 title claims abstract description 30
- 239000004814 polyurethane Substances 0.000 title claims abstract description 26
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 26
- 239000002966 varnish Substances 0.000 title claims abstract description 18
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 54
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 35
- -1 polysiloxanes Polymers 0.000 claims abstract description 31
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 29
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229920000058 polyacrylate Polymers 0.000 claims abstract description 23
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 20
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 18
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 18
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000012948 isocyanate Substances 0.000 claims abstract description 18
- 239000005543 nano-size silicon particle Substances 0.000 claims abstract description 18
- 229910021389 graphene Inorganic materials 0.000 claims abstract description 17
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 17
- OELQSSWXRGADDE-UHFFFAOYSA-N 2-methylprop-2-eneperoxoic acid Chemical compound CC(=C)C(=O)OO OELQSSWXRGADDE-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000006185 dispersion Substances 0.000 claims abstract description 16
- 239000002245 particle Substances 0.000 claims abstract description 15
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 13
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 13
- 239000010703 silicon Substances 0.000 claims abstract description 13
- 229920001577 copolymer Polymers 0.000 claims abstract description 11
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 9
- 239000000839 emulsion Substances 0.000 claims description 25
- 239000006210 lotion Substances 0.000 claims description 20
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 19
- 239000000377 silicon dioxide Substances 0.000 claims description 19
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 claims description 13
- 239000002518 antifoaming agent Substances 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 239000003999 initiator Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 9
- 239000000872 buffer Substances 0.000 claims description 9
- 229910000077 silane Inorganic materials 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 7
- 230000008878 coupling Effects 0.000 claims description 5
- 238000010168 coupling process Methods 0.000 claims description 5
- 238000005859 coupling reaction Methods 0.000 claims description 5
- 239000006071 cream Substances 0.000 claims description 5
- 238000006116 polymerization reaction Methods 0.000 claims description 5
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 claims description 4
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 2
- 229910003978 SiClx Inorganic materials 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000007822 coupling agent Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 238000010422 painting Methods 0.000 claims description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims 2
- 101100373011 Drosophila melanogaster wapl gene Proteins 0.000 claims 1
- 239000003377 acid catalyst Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 210000004483 pasc Anatomy 0.000 claims 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims 1
- 239000004408 titanium dioxide Substances 0.000 claims 1
- 239000000853 adhesive Substances 0.000 abstract description 6
- 230000001070 adhesive effect Effects 0.000 abstract description 6
- 229920005989 resin Polymers 0.000 abstract description 4
- 239000011347 resin Substances 0.000 abstract description 4
- 239000011159 matrix material Substances 0.000 abstract description 3
- 229940070721 polyacrylate Drugs 0.000 description 17
- 239000012153 distilled water Substances 0.000 description 16
- 238000003756 stirring Methods 0.000 description 15
- 238000013019 agitation Methods 0.000 description 13
- 230000002572 peristaltic effect Effects 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- 239000003995 emulsifying agent Substances 0.000 description 10
- 239000003973 paint Substances 0.000 description 8
- 239000011527 polyurethane coating Substances 0.000 description 8
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 7
- 239000000908 ammonium hydroxide Substances 0.000 description 7
- RCEAADKTGXTDOA-UHFFFAOYSA-N OS(O)(=O)=O.CCCCCCCCCCCC[Na] Chemical compound OS(O)(=O)=O.CCCCCCCCCCCC[Na] RCEAADKTGXTDOA-UHFFFAOYSA-N 0.000 description 6
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 6
- 229920000053 polysorbate 80 Polymers 0.000 description 6
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 6
- 235000019394 potassium persulphate Nutrition 0.000 description 6
- 238000010792 warming Methods 0.000 description 6
- 239000012298 atmosphere Substances 0.000 description 5
- 238000004945 emulsification Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 235000012239 silicon dioxide Nutrition 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000010025 steaming Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 239000012874 anionic emulsifier Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 239000012875 nonionic emulsifier Substances 0.000 description 2
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 2
- 238000004987 plasma desorption mass spectroscopy Methods 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000002604 ultrasonography Methods 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 1
- 206010054949 Metaplasia Diseases 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-N anhydrous cyanic acid Natural products OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 229960000935 dehydrated alcohol Drugs 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000015689 metaplastic ossification Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- VDGJOQCBCPGFFD-UHFFFAOYSA-N oxygen(2-) silicon(4+) titanium(4+) Chemical compound [Si+4].[O-2].[O-2].[Ti+4] VDGJOQCBCPGFFD-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000548 poly(silane) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
The invention discloses a kind of automobile varnish Si modification double-component waterborne polyurethane composite coatings and preparation method thereof, and composite coating is made of A and B component；Component A is silicon modified aqueous polyacrylate dispersion；B component includes hydrophilic isocyanate curing agent, graphene and auxiliary agent；Silicon modified aqueous polyacrylate dispersion includes methyl methacrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate and copolymer and silane-modified nano-silicon dioxide particle with double bond polysiloxanes；The composite coating uniformly introduces polysiloxanes and nano-silicon dioxide particle and graphene simultaneously in matrix resin, effectively increases adhesive force, the water resistance of composite coating, while increasing hardness and strength, is particularly suitable for automobile varnish.
Description
Technical field
The present invention relates to a kind of coating, and in particular to a kind of automobile varnish is multiple with organic-silicon-modified double-component waterborne polyurethane
Coating and preparation method thereof is closed, technical field of coatings is belonged to.
Background technique
Double-component waterborne polyurethane coating is generally by polyvalent alcohol lotion or the isocyanic acid of dispersion component and hydrophilic modifying
Ester curing agent component composition.There are aqueous polyhydroxy polycarboxylic acrylate raw material sources to enrich, advantage of lower cost, the feature of environmental protection are good
Weatherability, mechanical strength, glossiness and permeability of feature, especially its film etc. are had excellent performance, and are preferably poly- polynary
Alcohol lotion type.The isocyanate curing agent of it and hydrophilic modifying is with the carbamate after lacquering, contained in polyurethane structural
Key, urea bond, biuret and ester group etc. assign the excellent wearability of polyurethane coating film, flexibility, low temperature resistant and resistant to chemical media
Energy.Automotive clear coats need film to have excellent water resistance, glossiness and mechanical property.Due to emulsifier in conventional emulsion system
Presence, cause water paint form a film after water-fast effect it is poor, there is also certain gaps compared with solvent based coating, therefore having must
It is modified.There is using organo-silicon compound the solvent resistance for improving water-and acrylate in the prior art and hates
Aqueous and weatherability relevant report, as Chinese patent (publication number CN108690487A) discloses a kind of organic-silicon-modified double groups
Part polyurethane water-proof paint and preparation method thereof, it is solid using dimethyl silicone polymer (PDMS) and polyether units alcohol and isocyanates
Agent polymerization reaction forms the base polyurethane prepolymer for use as of the structure Han-Si-O-, then forms a film with cross-linking component cross-linking reaction.But the party
The PDMS that method uses includes saturated bond, and reaction efficiency is lower in modifying process.In addition, there are also improved using nano-particle material
The relevant report of Wear Resistance of Coating, as Chinese patent (publication number CN108676480A) provides a kind of double-component aqueous propylene
Sour polyurethane coating and preparation method thereof has synthesized water based acrylic resin by radical polymerization under solution system,
It is reacted again by the-OH of surface of nanometer zinc oxide with the-NCO in isocyanate curing agent, inorganic particle is grafted to curing agent
In, improve the wearability of coating.However the higher cost of nano zine oxide, Mohs' hardness is low, and it is consumed in curing agent
Active group influences solidification effect.
Summary of the invention
In view of the deficienciess of the prior art, the first purpose of this invention is to be to provide a kind of Si modification two-component water
Property polyurethane Composite Coating, the composite coating uniformly introduce polysiloxanes and nanometer titanium dioxide silicon grain simultaneously in matrix resin
Son etc., effectively increases adhesive force, the water resistance of composite coating, while increasing its hardness and strength, has preferable application
Prospect.
Second object of the present invention is to be to provide a kind of preparation of Si modification double-component waterborne polyurethane composite coating
Method, this method, can be as monomers and other acrylic acid by modifying double bond on octamethylcy-clotetrasiloxane (D4)
Monomer is copolymerized, and reaction efficiency is not only increased, and resin silicone content can be improved, and is conducive to the evenly dispersed of silane；
Meanwhile by carrying out organosilicon modification to inorganic nano silica surface, inorganic nano silica is improved in organic painting
Dispersibility in material enhances the mechanical property of film, and this method raw material is easy to get, and preparation process is simple, is conducive to industrial metaplasia
It produces.
In order to achieve the above technical purposes, the present invention provides a kind of automobile varnish Si modification double-component waterborne polyurethanes
Composite coating is made of A and B component；
The component A is silicon modified aqueous polyacrylate dispersion；
The B component includes hydrophilic isocyanate curing agent, graphene and auxiliary agent；
The silicon modified aqueous polyacrylate dispersion includes methyl methacrylate, butyl acrylate, styrene, propylene
Acid, methacrylic acid β hydroxy methacrylate and copolymer and silane-modified nano-silicon dioxide particle with double bond polysiloxanes.
Preferred scheme, it is described anti-by octamethylcy-clotetrasiloxane and the silane coupling agent with double bond with double bond polysiloxanes
It should obtain.The preferred octamethylcy-clotetrasiloxane of the present invention carrys out anamorphic zone double bond polysiloxanes, and octamethylcy-clotetrasiloxane is with respect to it
His polysilane has the characteristics that silicone content is moderate, and the polysiloxanes that gel fraction is smaller, more stable can be prepared with coupling agent open loop.
Preferred scheme, the silane-modified nano-silicon dioxide particle is by silane coupling agent and nano-silica with amino
SiClx reacts to obtain.Condensation reaction is carried out using the amino of silane coupling agent and the active group of silica surface.
Preferably the silane coupling agent with double bond is silane coupling A 171.
Preferably the silane coupling agent with amino is Silane coupling agent KH550.
Preferred scheme, methyl methacrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxyl second
Ester and mass ratio with double bond polysiloxanes are (15~20): (8~12): (8~12): (0.5~1.5): (4~7.5):
(1.25~2.5).
The dosage of preferred scheme, graphene and auxiliary agent be hydrophilic isocyanate curing agent quality 2.5%~
9%.The present invention improves the mechanical property after composite coating solidifies, the special arrangement side of the carbon atom of graphene using graphene
Formula, thus have excellent hardness and preferable flexibility, the mechanical property of film can be effectively improved by being entrained in composite coating
Energy.
Preferred scheme, the auxiliary agent include defoaming agent and levelling agent；The mass ratio of defoaming agent and levelling agent is (1~2):
(1~1.5).Defoaming agent J0401 is purchased from Shenzhen Jitian's chemical industry, and levelling agent BYK333 is purchased from Dongguan power victory chemical industry.
Preferred scheme, component A and B component mass ratio are (5~6): 1；Wherein component A solid content is 35%~55%.
Preferably 45~50%.
The present invention also provides a kind of automobile varnish preparation method of Si modification double-component waterborne polyurethane composite coating,
Itself the following steps are included:
1) octamethylcy-clotetrasiloxane is added dropwise in the lotion containing catalyst with the silane coupling agent with double bond and is reacted, obtained
To band double bond polysiloxanes；
2) silane coupling agent with amino is added dropwise in nano silicon dioxide dispersion and is reacted, obtain silane-modified nanometer
Silicon dioxide granule；
3) part is contained into methyl methacrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate
Lotion be added dropwise in the water phase containing initiator and buffer and carry out prepolymerization, then to add in prepolymerization system initiator gentle
After electuary, remaining part is contained into methyl methacrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxyl second
The lotion of ester is added dropwise in prepolymerization system together with band double bond polysiloxanes and carries out polymerization reaction, obtains copolymer emulsion；
4) copolymer emulsion is uniformly mixed with silane-modified nano-silicon dioxide particle to get silicon modified aqueous polypropylene
Acid esters lotion；
5) hydrophilic isocyanate curing agent, graphene and auxiliary agent are added in silicon modified aqueous polyacrylate dispersion,
Be uniformly mixed to get.
Octamethylcy-clotetrasiloxane is added dropwise to silane coupling A 171 and urges containing dodecyl benzene sulfonic acid by preferred scheme
In the lotion of agent, 6~18h is reacted at a temperature of 70~90 DEG C, obtains band double bond polysiloxanes；Octamethylcy-clotetrasiloxane with
The mass ratio of silane coupling A 171 is (2~4): 2.
Preferred scheme, Silane coupling agent KH550 is added dropwise in nano silicon dioxide dispersion, in 30~50 DEG C of temperature
Under carry out 6~18h of reaction, obtain silane-modified nano-silicon dioxide particle；Silane coupling agent KH550 and nano silica
Mass ratio is (3~4): 1.
1/4~1/2 volume is contained methyl methacrylate, butyl acrylate, styrene, acrylic acid, first by preferred scheme
The lotion of base propenoic acid beta hydroxy methacrylate is added dropwise in the water phase containing initiator and buffer in 70~90 DEG C of progress prepolymerizations 0.5
~3.5h, then after adding initiator and buffer in prepolymerization system, remaining part is contained into methyl methacrylate, acrylic acid
Butyl ester, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate lotion with band double bond polysiloxanes together be added dropwise to prepolymerization
0.5~4.5h of polymerization reaction is carried out in system, obtains copolymer emulsion.
The mass ratio of copolymer emulsion and silane-modified nano-silicon dioxide particle is 20:(0.1~0.4).
Hydrophilic isocyanate curing agent of the invention is directly boughtN3800 aliphatic isocyanates
Curing agent.Its NCO content is 11.0 ± 0.5%, and (23 DEG C) of viscosity are 6000 ± 1200mPas, and purchase address is that Guangzhou sky is firm
Chemical Industry Science Co., Ltd.
Graphene of the invention includes graphene oxide, graphite alkane, nitrogen-doped graphene etc..
The emulsifier used in emulsion polymerization process of the present invention compounds for anionic emulsifier/nonionic emulsifier,
Wherein anionic emulsifier be one of dodecyl sodium sulfate, lauryl sodium sulfate, neopelex or
Several, nonionic emulsifier is one or both of Tween 80, allyloxy hydroxypropyl azochlorosulfonate acid sodium.Emulsifier is poly-
Close the 4% of monomer gross mass.
Initiator of the invention is at least one of peroxidating class thermal initiator potassium peroxydisulfate, ammonium persulfate, and dosage is
The 0.9% of polymerized monomer gross mass.
A kind of preparation of automobile varnish of the invention Si modification double-component waterborne polyurethane composite coating includes following tool
Body step:
(1) synthesis with double bond polysiloxanes: emulsifier is dissolved in the water, and water-bath is to 80 DEG C under the conditions of magnetic agitation.
D4 and A171 is instilled in beaker in 1h with the ratio of mass ratio 3:2, is added catalyst dodecyl benzene sulfonic acid (DBSA), after
Continuous reaction 12h.It is cooled to after room temperature after adjusting pH to neutrality with ammonium hydroxide and is made.
(2) surface of nano silica is modified: a certain amount of nano silica is taken, is scattered in dehydrated alcohol,
Water-bath is to 40 DEG C under the conditions of magnetic agitation.KH550 is instilled into beaker in 1h, the reaction was continued 12h.After the reaction was completed by dispersion liquid
Centrifugation is put into the dry 12h of vacuum oven afterwards twice.
(3) initiator, buffer and distilled water the synthesis of poly acrylate composite emulsion: are added in three-necked flask.By first
Base methyl acrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate, which are added in emulsifier aqueous solution, to be added
Speed 1~2h of stirring is at uniform lotion.1/3 pre-emulsion is instilled in three-necked flask by peristaltic pump, stirring is warming up to 80 DEG C.To
The reaction was continued 1h after pre-emulsion drips off after adding quantitative initiator and buffer, then will be synthesized in remaining pre-emulsion and (1)
Band double bond polysiloxanes instills flask, drips off subsequent continuation of insurance temperature 1h.Be down to room temperature to it after the reaction was completed, with ammonium hydroxide adjust pH to
It is neutral.It disperses the modified manometer silicon dioxide in (2) in made lotion, and 0.5~1h is stirred by ultrasonic.
(4) preparation of dual-component coating: being added the polyacrylic acid multiple emulsion synthesized in (3) in three-necked flask, machinery stirs
Hydrophilically modified polyisocyanates curing agent, graphene, defoaming agent, coalescing agent and suitable quantity of water are added under the conditions of mixing.
Compared with the prior art, technical solution of the present invention bring advantageous effects:
Si modification double-component waterborne polyurethane composite coating provided by the invention uniformly introduces in matrix resin simultaneously
Polysiloxanes and nano-silicon dioxide particle and graphene, using the Si-O key in organosilicon have bond energy larger surface tension compared with
Small feature, the adhesive force and water resistance of Lai Tigao coating, and effectively mentioned by introducing nano-silicon dioxide particle and graphene
High hardness and strength of coating, therefore composite coating effectively increases its adhesive force, water resistance, while increasing hardness and strong
Degree is particularly suitable for automobile varnish.
The present invention is by modifying double bond on octamethylcy-clotetrasiloxane (D4), so as to directly be incited somebody to action by copolymerization process
Octamethylcy-clotetrasiloxane is introduced into acrylic copolymer, not only improves the reaction efficiency that silane introduces process, to improve tree
Rouge silicone content, and be conducive to the evenly dispersed of silane.
The present invention utilizes organosilan and organic tree by carrying out organosilan modification to inorganic nano silica surface
The good feature of lipid phase capacitive improves dispersibility of the inorganic nano silica in organic coating, enhances the mechanics of film
Performance.
Si modification double-component waterborne polyurethane composite coating preparation method of the invention is simple, and raw material is easy to get, at low cost, has
Conducive to large-scale application.
Detailed description of the invention
Fig. 1 is the figure of organosilicon polyacrylate dispersion TEM obtained by the present invention.
Fig. 2 is the infrared comparison diagram of rear nano silica before modified of KH550 obtained by the present invention.
Specific embodiment
Content that following embodiment is further intended to that the present invention will be described in detail, rather than limit the claims in the present invention and protect model
It encloses.
Embodiment 1
By 18 parts of methyl methacrylates, 10 parts of butyl acrylates, 10 parts of styrene, 4 parts of methacrylic acid β hydroxyl second
Ester, 1.3 parts of lauryl sodium sulfate of 1 part of acrylic acid and emulsifier, 0.7 part of Tween 80 are added in beaker, add 20mL steaming
Distilled water, 0.5~1h of magnetic agitation to complete emulsification.0.13 part is added in the three-necked flask that one is equipped with agitating paddle, condenser
Potassium peroxydisulfate, 0.05 part of sodium bicarbonate and 10mL distilled water, nitrogen is passed through under atmosphere heating stirring to 75 DEG C, then takes 1/3 pre- cream
Liquid is instilled in flask with peristaltic pump, and 1~1.5h is dripped off, and is warming up to 80 DEG C and is kept the temperature 1h.Then 0.25 part of persulfuric acid is added simultaneously
Potassium, and remaining 2/3 pre-emulsion is instilled into flask by peristaltic pump, 2~2.5h is dripped off and is kept the temperature 1h.Finally it is cooled to room temperature addition
It is 7~8 that ammonium hydroxide, which adjusts pH value, obtains conventional polypropylene acid esters lotion.
Embodiment 2
By 18 parts of methyl methacrylates, 10 parts of butyl acrylates, 10 parts of styrene, 1 part of acrylic acid, 4 parts of metering systems
1.3 parts of lauryl sodium sulfate of sour β hydroxy methacrylate and emulsifier, 0.7 part of Tween 80 are added in beaker, add 20mL steaming
Distilled water, 0.5~1h of magnetic agitation to complete emulsification.0.13 part is added in the three-necked flask that one is equipped with agitating paddle, condenser
Potassium peroxydisulfate, 0.05 part of sodium bicarbonate and 10mL distilled water, nitrogen is passed through under atmosphere heating stirring to 75 DEG C, then takes 1/3 pre- cream
Liquid is instilled in flask with peristaltic pump, and 1~1.5h is dripped off, and is warming up to 80 DEG C and is kept the temperature 1h.Then 0.25 part of persulfuric acid is added simultaneously
Potassium, and 1.7 parts of homemade band double bond polysiloxanes and remaining 2/3 pre-emulsion are instilled into flask by peristaltic pump, 2~2.5h is dripped off
And keep the temperature 1h.Finally being cooled to room temperature and ammonium hydroxide is added to adjust pH value is 7~8, obtains silicone-modified polyacrylate lotion.
Embodiment 3
By 18 parts of methyl methacrylates, 10 parts of butyl acrylates, 10 parts of styrene, 1 part of acrylic acid, 4 parts of metering systems
1.3 parts of lauryl sodium sulfate of sour β hydroxy methacrylate and emulsifier, 0.7 part of Tween 80 are added in beaker, add 20mL distillation
Water, 0.5~1h of magnetic agitation to complete emulsification.0.13 part of mistake is added in the three-necked flask that one is equipped with agitating paddle, condenser
Potassium sulfate, 0.05 part of sodium bicarbonate and 10mL distilled water, nitrogen is passed through under atmosphere heating stirring to 75 DEG C, then takes 1/3 pre-emulsion,
It is instilled in flask with peristaltic pump, 1~1.5h is dripped off, and is warming up to 80 DEG C and is kept the temperature 1h.Then 0.25 part of potassium peroxydisulfate is added simultaneously,
And 3 parts of homemade band double bond polysiloxanes and remaining 2/3 pre-emulsion are instilled into flask by peristaltic pump, 2~2.5h is dripped off and is protected
Warm 1h.Finally being cooled to room temperature and ammonium hydroxide is added to adjust pH value is 7~8, obtains silicone-modified polyacrylate lotion.
Embodiment 4
By 18 parts of methyl methacrylates, 10 parts of butyl acrylates, 10 parts of styrene, 1 part of acrylic acid, 4 parts of metering systems
1.3 parts of lauryl sodium sulfate of sour β hydroxy methacrylate and emulsifier, 0.7 part of Tween 80 are added in beaker, add 20mL steaming
Distilled water, 0.5~1h of magnetic agitation to complete emulsification.0.13 part is added in the three-necked flask that one is equipped with agitating paddle, condenser
Potassium peroxydisulfate, 0.05 part of sodium bicarbonate and 10mL distilled water, nitrogen is passed through under atmosphere heating stirring to 75 DEG C, then takes 1/3 pre- cream
Liquid is instilled in flask with peristaltic pump, and 1~1.5h is dripped off, and is warming up to 80 DEG C and is kept the temperature 1h.Then 0.25 part of persulfuric acid is added simultaneously
Potassium, and 1.7 parts of homemade band double bond polysiloxanes and remaining 2/3 pre-emulsion are instilled into flask by peristaltic pump, 2~2.5h is dripped off
And keep the temperature 1h.Finally being cooled to room temperature and ammonium hydroxide is added to adjust pH value is 7~8.
20 parts of self-control organosilicon polyacrylate dispersions are taken, 0.2 part of modified manometer silicon dioxide is added under ultrasound condition,
Up to Si modification poly acrylate composite emulsion after 0.5~1h of stirring.
Embodiment 5
By 18 parts of methyl methacrylates, 10 parts of butyl acrylates, 10 parts of styrene, 1 part of acrylic acid, 4 parts of metering systems
1.3 parts of lauryl sodium sulfate of sour β hydroxy methacrylate and emulsifier, 0.7 part of Tween 80 are added in beaker, add 20mL steaming
Distilled water, 0.5~1h of magnetic agitation to complete emulsification.0.13 part is added in the three-necked flask that one is equipped with agitating paddle, condenser
Potassium peroxydisulfate, 0.05 part of sodium bicarbonate and 10mL distilled water, nitrogen is passed through under atmosphere heating stirring to 75 DEG C, then takes 1/3 pre- cream
Liquid is instilled in flask with peristaltic pump, and 1~1.5h is dripped off, and is warming up to 80 DEG C and is kept the temperature 1h.Then 0.25 part of persulfuric acid is added simultaneously
Potassium, and 1.7 parts of homemade band double bond polysiloxanes and remaining 2/3 pre-emulsion are instilled into flask by peristaltic pump, 2~2.5h is dripped off
And keep the temperature 1h.Finally being cooled to room temperature and ammonium hydroxide is added to adjust pH value is 7~8.
20 parts of self-control organosilicon polyacrylate dispersions are taken, 0.6 part of modified manometer silicon dioxide is added under ultrasound condition,
Up to Si modification poly acrylate composite emulsion after 0.5~1h of stirring.
Embodiment 6
Take 3.5 parts of hydrophilic isocyanate curing agent in beaker, by routine made in embodiment 1 under the conditions of magnetic agitation
Beaker is added in polyacrylate dispersion, adjusts viscosity depending on concrete condition distilled water.0.1 part of defoaming agent, 0.05 part of levelling is added
Agent is stirred after 0.5h up to double-component waterborne polyurethane coating.
Embodiment 7
It take 3.5 parts of hydrophilic isocyanate curing agent in beaker, is formed in embodiment 2 under the conditions of magnetic agitation
Beaker is added in machine Si modification polyacrylate dispersion, adjusts viscosity depending on concrete condition distilled water.Be added 0.1 part of defoaming agent,
0.05 part of levelling agent stirs after 0.5h up to organic-silicon-modified double-component waterborne polyurethane coating.
Embodiment 8
It take 3.5 parts of hydrophilic isocyanate curing agent in beaker, is formed in embodiment 3 under the conditions of magnetic agitation
Beaker is added in machine Si modification polyacrylate dispersion, adjusts viscosity depending on concrete condition distilled water.Be added 0.1 part of defoaming agent,
0.05 part of levelling agent stirs after 0.5h up to organic-silicon-modified double-component waterborne polyurethane coating.
Embodiment 9
It takes 3.5 parts of hydrophilic isocyanate curing agent in beaker, will be made silicon in embodiment 4 under the conditions of magnetic agitation
Beaker is added in modified polyacrylate multiple emulsion, adjusts viscosity depending on concrete condition distilled water.Be added 0.1 part of defoaming agent,
0.05 part of levelling agent stirs after 0.5h up to Si modification double-component waterborne polyurethane composite coating.
Embodiment 10
It takes 3.5 parts of hydrophilic isocyanate curing agent in beaker, will be made silicon in embodiment 5 under the conditions of magnetic agitation
Beaker is added in modified polyacrylate multiple emulsion, adjusts viscosity depending on concrete condition distilled water.Be added 0.1 part of defoaming agent,
0.05 part of levelling agent stirs after 0.5h up to Si modification double-component waterborne polyurethane composite coating.
Embodiment 11
It takes 3.5 parts of hydrophilic isocyanate curing agent in beaker, will be made silicon in embodiment 4 under the conditions of magnetic agitation
Beaker is added in modified polyacrylate multiple emulsion, adjusts viscosity depending on concrete condition distilled water.0.6 part of graphene, 0.1 is added
Part defoaming agent, 0.05 part of levelling agent stir after 0.5h up to Si modification double-component waterborne polyurethane composite coating.
5~10 gained double-component waterborne polyurethane coating of above-described embodiment is surveyed with paint field common testing methods
Examination, the results are shown in Table 1:
1 test result of table
As shown in Table 1, embodiment 7 has passed through 96h water resistance test, and water resistance and adhesive force are superior to embodiment 6, explanation
The addition of organosilicon improves the water resistance and adhesive force of paint film, and the Storage period of embodiment 8 is short compared with embodiment 7, illustrates organosilicon
Excessive be added will affect its stability；The hardness of paint film of embodiment 7,9,11 is gradually increased, and illustrates improved silica and graphite
The addition of alkene improves the hardness of paint film, and the paint film appearance out-of-flatness of embodiment 10 has granular sensation, illustrates that silica excessively adds
Add and will cause reunion, influences appearance of film.The present invention uses obtained by self-control polysiloxanes and KH550 modified manometer silicon dioxide
Si modification double-component waterborne polyurethane composite coating, while guaranteeing stability, the water resistance of paint film, hardness, attachment
Power, which suffers from, to be obviously improved.
Above embodiments are the general embodiment of the present invention, but embodiments of the present invention are not limited to above-mentioned implementation
Example, others are any should all without departing from made various changes, improvement, combination under spiritual essence and principle range of the invention etc.
For equivalent substitute mode, it is included within the scope of the present invention.
Claims (10)
1. a kind of automobile varnish Si modification double-component waterborne polyurethane composite coating, it is characterised in that: be made of A and B component；
The component A is silicon modified aqueous polyacrylate dispersion；
The B component includes hydrophilic isocyanate curing agent, graphene and auxiliary agent；
The silicon modified aqueous polyacrylate dispersion include methyl methacrylate, butyl acrylate, styrene, acrylic acid,
Methacrylic acid β hydroxy methacrylate and copolymer and silane-modified nano-silicon dioxide particle with double bond polysiloxanes.
2. a kind of automobile varnish according to claim 1 Si modification double-component waterborne polyurethane composite coating, feature
It is:
It is described to react to obtain with the silane coupling agent with double bond by octamethylcy-clotetrasiloxane with double bond polysiloxanes；
The silane-modified nano-silicon dioxide particle is obtained by the silane coupling agent with amino and nanometer titanium dioxide pasc reaction；
The silane coupling agent with double bond is silane coupling A 171；
The silane coupling agent with amino is Silane coupling agent KH550.
3. a kind of automobile varnish according to claim 1 Si modification double-component waterborne polyurethane composite coating, feature
It is: methyl methacrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate and with the poly- silicon of double bond
The mass ratio of oxygen alkane is (15~20): (8~12): (8~12): (0.5~1.5): (4~7.5): (1.25~2.5).
4. a kind of automobile varnish according to claim 1 Si modification double-component waterborne polyurethane composite coating, feature
Be: the dosage of graphene and auxiliary agent is the 2.5%~9% of hydrophilic isocyanate curing agent quality.
5. a kind of automobile varnish according to claim 4 Si modification double-component waterborne polyurethane composite coating, feature
Be: the auxiliary agent includes defoaming agent and levelling agent；The mass ratio of defoaming agent and levelling agent is (1~2): (1~1.5).
6. described in any item a kind of automobile varnishs compound painting of Si modification double-component waterborne polyurethane according to claim 1~5
Material, it is characterised in that: component A is (5~6) with B component mass ratio: 1；Wherein, component A solid content is 35%~55%.
7. a kind of described in any item automobile varnish Si modification double-component waterborne polyurethane composite coatings of claim 1~6
Preparation method, it is characterised in that: the following steps are included:
1) octamethylcy-clotetrasiloxane is added dropwise in the lotion containing catalyst with the silane coupling agent with double bond and is reacted, obtain band
Double bond polysiloxanes；
2) silane coupling agent with amino is added dropwise in nano silicon dioxide dispersion and is reacted, obtain silane-modified nano-silica
SiClx particle；
3) by part containing methyl methacrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate cream
Drop adds to and carries out prepolymerization in the water phase containing initiator and buffer, then adds initiator and buffer in prepolymerization system
Afterwards, by remaining part containing methyl methacrylate, butyl acrylate, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate
Lotion is added dropwise in prepolymerization system together with band double bond polysiloxanes and carries out polymerization reaction, obtains copolymer emulsion；
4) copolymer emulsion is uniformly mixed with silane-modified nano-silicon dioxide particle to get silicon modified aqueous polyacrylate
Lotion；
5) hydrophilic isocyanate curing agent, graphene and auxiliary agent, mixing are added in silicon modified aqueous polyacrylate dispersion
Uniformly to get.
8. a kind of preparation side of automobile varnish Si modification double-component waterborne polyurethane composite coating according to claim 7
Method, it is characterised in that: octamethylcy-clotetrasiloxane and silane coupling A 171 are added dropwise to containing dodecylbenzene sulfonic acid catalyst
Lotion in, at a temperature of 70~90 DEG C react 6~18h, obtain band double bond polysiloxanes；Octamethylcy-clotetrasiloxane and silane
The mass ratio of coupling agent A171 is (2~4): 2.
9. a kind of preparation side of automobile varnish Si modification double-component waterborne polyurethane composite coating according to claim 7
Method, it is characterised in that: Silane coupling agent KH550 is added dropwise in nano silicon dioxide dispersion, at a temperature of 30~50 DEG C into
Row 6~18h of reaction, obtains silane-modified nano-silicon dioxide particle；The quality of Silane coupling agent KH550 and nano silica
Than for (3~4): 1.
10. a kind of preparation of automobile varnish Si modification double-component waterborne polyurethane composite coating according to claim 7
Method, it is characterised in that: 1/4~1/2 volume is contained into methyl methacrylate, butyl acrylate, styrene, acrylic acid, methyl
The lotion of propenoic acid beta hydroxy methacrylate be added dropwise in the water phase containing initiator and buffer 70~90 DEG C of progress prepolymerizations 0.5~
3.5h, then after adding initiator and buffer in prepolymerization system, remaining part is contained into methyl methacrylate, acrylic acid fourth
Ester, styrene, acrylic acid, methacrylic acid β hydroxy methacrylate lotion with band double bond polysiloxanes together be added dropwise to pre-polymers
0.5~4.5h of polymerization reaction is carried out in system, obtains copolymer emulsion；Copolymer emulsion and silane-modified nano-silicon dioxide particle
Mass ratio be 20:(0.1~0.4).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910094774.8A CN109762454B (en) | 2019-01-31 | 2019-01-31 | Preparation method of silicon-modified two-component waterborne polyurethane composite coating for automobile varnish |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910094774.8A CN109762454B (en) | 2019-01-31 | 2019-01-31 | Preparation method of silicon-modified two-component waterborne polyurethane composite coating for automobile varnish |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN109762454A true CN109762454A (en) | 2019-05-17 |
| CN109762454B CN109762454B (en) | 2020-02-14 |
Family
ID=66455632
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201910094774.8A Expired - Fee Related CN109762454B (en) | 2019-01-31 | 2019-01-31 | Preparation method of silicon-modified two-component waterborne polyurethane composite coating for automobile varnish |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN109762454B (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110698614A (en) * | 2019-10-29 | 2020-01-17 | 上海雅运新材料有限公司 | Core-shell (methyl) acrylate copolymer particle emulsion, preparation method thereof and fabric deepening agent composition |
| CN110724430A (en) * | 2019-09-05 | 2020-01-24 | 深圳市安品有机硅材料有限公司 | Water-based composite coating material and preparation method and application thereof |
| CN111394039A (en) * | 2020-05-21 | 2020-07-10 | 重庆索梦得新材料科技有限公司 | Graphene nano three-proofing adhesive and preparation method thereof |
| CN112280043A (en) * | 2020-10-30 | 2021-01-29 | 三棵树(上海)新材料研究有限公司 | Silicon dioxide/polyacrylate/polysiloxane composite emulsion, preparation method and application thereof |
| CN112726273A (en) * | 2021-01-30 | 2021-04-30 | 汕头市鑫源化工科技有限公司 | Water-based high-gloss paint and preparation method thereof |
| CN113416482A (en) * | 2020-11-14 | 2021-09-21 | 深圳市蓝博环保科技有限公司 | Waterborne polyurethane coating |
| CN114479707A (en) * | 2022-02-26 | 2022-05-13 | 浙江世窗光学薄膜制造有限公司 | Polyurethane multilayer film and preparation method thereof |
| CN115340798A (en) * | 2022-09-15 | 2022-11-15 | 浙江鱼童新材料股份有限公司 | High-solid acrylic resin coating |
| CN115368813A (en) * | 2021-05-19 | 2022-11-22 | 黄建发 | Scratch-resistant double-component polyurethane varnish |
| CN115490907A (en) * | 2022-11-02 | 2022-12-20 | 南宁斤美新材料科技有限公司 | Preparation method of high-temperature-resistant oil-stain-resistant composite plastic |
| CN116023852A (en) * | 2022-11-28 | 2023-04-28 | 江苏金陵特种涂料有限公司 | Ultra-early water-resistant silicon modified waterborne polyurethane coating and preparation method thereof |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103320000A (en) * | 2013-06-17 | 2013-09-25 | 玖青涂料（上海）有限公司 | Water-based two-component fluorosilicone acrylic anticorrosive paint and preparation method thereof |
| CN105949396A (en) * | 2016-05-12 | 2016-09-21 | 武汉赫斯特涂层材料股份有限公司 | Water-based polysiloxane resin and preparation method thereof |
| CN108841216A (en) * | 2018-06-01 | 2018-11-20 | 厦门派探特环保科技有限公司 | A kind of environmental protection graphene high durable automobile water paint and preparation method thereof |
| CN109135533A (en) * | 2018-07-26 | 2019-01-04 | 深圳市莱莉雅环保科技有限公司 | Scintilla aqueous automobile interior paint, preparation process and spraying method with graphene |
| CN109266187A (en) * | 2018-08-10 | 2019-01-25 | 恒力盛泰（厦门）石墨烯科技有限公司 | A kind of heat radiation coating and preparation method containing isocyanate-modified graphene |
-
2019
- 2019-01-31 CN CN201910094774.8A patent/CN109762454B/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103320000A (en) * | 2013-06-17 | 2013-09-25 | 玖青涂料（上海）有限公司 | Water-based two-component fluorosilicone acrylic anticorrosive paint and preparation method thereof |
| CN105949396A (en) * | 2016-05-12 | 2016-09-21 | 武汉赫斯特涂层材料股份有限公司 | Water-based polysiloxane resin and preparation method thereof |
| CN108841216A (en) * | 2018-06-01 | 2018-11-20 | 厦门派探特环保科技有限公司 | A kind of environmental protection graphene high durable automobile water paint and preparation method thereof |
| CN109135533A (en) * | 2018-07-26 | 2019-01-04 | 深圳市莱莉雅环保科技有限公司 | Scintilla aqueous automobile interior paint, preparation process and spraying method with graphene |
| CN109266187A (en) * | 2018-08-10 | 2019-01-25 | 恒力盛泰（厦门）石墨烯科技有限公司 | A kind of heat radiation coating and preparation method containing isocyanate-modified graphene |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110724430A (en) * | 2019-09-05 | 2020-01-24 | 深圳市安品有机硅材料有限公司 | Water-based composite coating material and preparation method and application thereof |
| CN110724430B (en) * | 2019-09-05 | 2021-10-26 | 深圳市安品有机硅材料有限公司 | Water-based composite coating material and preparation method and application thereof |
| CN110698614A (en) * | 2019-10-29 | 2020-01-17 | 上海雅运新材料有限公司 | Core-shell (methyl) acrylate copolymer particle emulsion, preparation method thereof and fabric deepening agent composition |
| CN111394039A (en) * | 2020-05-21 | 2020-07-10 | 重庆索梦得新材料科技有限公司 | Graphene nano three-proofing adhesive and preparation method thereof |
| CN112280043B (en) * | 2020-10-30 | 2022-06-07 | 三棵树(上海)新材料研究有限公司 | Silicon dioxide/polyacrylate/polysiloxane composite emulsion, preparation method and application thereof |
| CN112280043A (en) * | 2020-10-30 | 2021-01-29 | 三棵树(上海)新材料研究有限公司 | Silicon dioxide/polyacrylate/polysiloxane composite emulsion, preparation method and application thereof |
| CN113416482A (en) * | 2020-11-14 | 2021-09-21 | 深圳市蓝博环保科技有限公司 | Waterborne polyurethane coating |
| CN112726273A (en) * | 2021-01-30 | 2021-04-30 | 汕头市鑫源化工科技有限公司 | Water-based high-gloss paint and preparation method thereof |
| CN112726273B (en) * | 2021-01-30 | 2023-08-22 | 汕头市鑫源化工科技有限公司 | Water-based high-gloss paint and preparation method thereof |
| CN115368813A (en) * | 2021-05-19 | 2022-11-22 | 黄建发 | Scratch-resistant double-component polyurethane varnish |
| CN115368813B (en) * | 2021-05-19 | 2023-12-19 | 广东百川化工有限公司 | Scratch-resistant bi-component polyurethane varnish |
| CN114479707A (en) * | 2022-02-26 | 2022-05-13 | 浙江世窗光学薄膜制造有限公司 | Polyurethane multilayer film and preparation method thereof |
| CN114479707B (en) * | 2022-02-26 | 2023-03-14 | 浙江世窗光学薄膜制造有限公司 | Polyurethane multilayer film and preparation method thereof |
| CN115340798A (en) * | 2022-09-15 | 2022-11-15 | 浙江鱼童新材料股份有限公司 | High-solid acrylic resin coating |
| CN115490907A (en) * | 2022-11-02 | 2022-12-20 | 南宁斤美新材料科技有限公司 | Preparation method of high-temperature-resistant oil-stain-resistant composite plastic |
| CN115490907B (en) * | 2022-11-02 | 2023-07-28 | 揭阳市冠业塑料制品有限公司 | Preparation method of high Wen Fangyou dirt-resistant composite plastic |
| CN116023852A (en) * | 2022-11-28 | 2023-04-28 | 江苏金陵特种涂料有限公司 | Ultra-early water-resistant silicon modified waterborne polyurethane coating and preparation method thereof |
| CN116023852B (en) * | 2022-11-28 | 2023-10-13 | 江苏金陵特种涂料有限公司 | Ultra-early water-resistant silicon modified waterborne polyurethane coating and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN109762454B (en) | 2020-02-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN109762454A (en) | A kind of preparation method of automobile varnish Si modification double-component waterborne polyurethane composite coating | |
| CN102993782B (en) | Preparation method of polyurethane acrylate oligomer surface modified silica | |
| CN102199239B (en) | Preparation method for acrylic acid microemulsion with self-crosslinking core-shell structure | |
| CN107573474B (en) | Silicone-modified waterborne polyurethane-acrylic resin emulsion and preparation method thereof | |
| CN103665269B (en) | A kind of preparation method of amphiphilic acrylate copolymer surface graft modification nano silicon | |
| CN102977282B (en) | Preparation method of anionic organic-solvent-free and emulsifier-free polyurethane microemulsion | |
| CN103396518B (en) | A kind of organic-silicon-modified waterborne acrylic paint and preparation method thereof | |
| CN105273557B (en) | A kind of aqueous woodware paint and preparation method thereof | |
| Parvate et al. | Advances in self-crosslinking of acrylic emulsion: What we know and what we would like to know | |
| CN101270225B (en) | Method for preparing binary dispersion composite emulsion of polyurethane acrylic acid | |
| CN104744639B (en) | A kind of preparation method of organic-silicon-modified normal-temperature multiple self-cross-linking epoxy resin emulsion | |
| CN109868026A (en) | A kind of Silicone-Modified Acrylate Resin and preparation method thereof and the hydrophobic weather-proof acrylic resin modified coating of sustained release | |
| CN101831230A (en) | Method for preparing polyacrylate/nano-SiO2 compound coating agent by using reactive emulsifier | |
| CN103602193A (en) | Priming paint for water-borne heavy anti-corrosion coating and preparation method thereof | |
| CN103980792B (en) | A kind of room temperature ketone hydrazine crosslinking VOC free water paint and preparation method thereof | |
| CN103980791B (en) | Waterborne organic silicon polyurethane-polyacrylate nano hybridization coating that a kind of VOC free is chitin modified and preparation method thereof | |
| CN109476789A (en) | Water-borne dispersions and application thereof | |
| JP2015514155A (en) | A polymer that can be produced by emulsion polymerization of functionalized polyurethane nanoparticles and a radical curable monomer, a method for producing the polymer, and use of the polymer. | |
| CN103709884B (en) | Organic-silicon-modified waterbased urethane priming paint of a kind of VOC free and preparation method thereof | |
| CN108795166A (en) | A kind of high abrasion-resistant environmental protection water-based gloss oil and preparation method thereof | |
| CN110229302A (en) | A kind of aqueous polyurethane emulsion and preparation method thereof of side chain silicon atoms | |
| CN106634785A (en) | Method for preparing aqueous polyurethane adhesive with good water resistance | |
| Elizalde et al. | Synthesis of butyl acrylate–styrene–TMI latexes and their application as water-based coatings | |
| CN103161082A (en) | Organosilicone modification pigment printing adhesion agent and preparation method thereof | |
| KR20090038271A (en) | Polyurethane-acrylate hybrid resin contained plastisol compound |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20200214 |